SERPINF2 Chromosome 17

Serpin family F member 2
9 variants 9 Health Risk

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What This Gene Does
This gene encodes a member of the serpin family of serine protease inhibitors. The protein is a major inhibitor of plasmin, which degrades fibrin and various other proteins. Consequently, the proper function of this gene has a major role in regulating the blood clotting pathway. Mutations in this gene result in alpha-2-plasmin inhibitor deficiency, which is characterized by severe hemorrhagic diathesis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]
Gene Info
Gene Group
Serpin peptidase inhibitors
Locus Type
gene with protein product
Location
17p13.3
Ensembl
ENSG00000167711
Associated Conditions (2)
Alpha-2-plasmin inhibitor deficiency
Abnormal bleeding
Key Variants
All Variants (9)
RSID Category Clinical Significance Conditions
RS142502473 Health Risk Conflicting classifications of pathogenicity
RS144824741 Health Risk Conflicting classifications of pathogenicity
RS144890920 Health Risk Conflicting classifications of pathogenicity
RS201542762 Health Risk Conflicting classifications of pathogenicity
RS200885603 Health Risk Likely pathogenic
RS121965061 Health Risk Pathogenic Alpha-2-plasmin inhibitor deficiency, Alpha-2-plasmin inhibitor deficiency
RS121965062 Health Risk Pathogenic Alpha-2-plasmin inhibitor deficiency, Alpha-2-plasmin inhibitor deficiency
RS1597325785 Health Risk Pathogenic Abnormal bleeding, Abnormal bleeding
RS2543443583 Health Risk Pathogenic Alpha-2-plasmin inhibitor deficiency, Alpha-2-plasmin inhibitor deficiency
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